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LINC01047 long intergenic non-protein coding RNA 1047 [ Homo sapiens (human) ]

Gene ID: 105616982, updated on 23-Nov-2021

Summary

Official Symbol
LINC01047provided by HGNC
Official Full Name
long intergenic non-protein coding RNA 1047provided by HGNC
Primary source
HGNC:HGNC:49041
See related
Ensembl:ENSG00000232225
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See LINC01047 in Genome Data Viewer
Location:
13q31.2
Exon count:
5
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 13 NC_000013.11 (89214847..89236890, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (89867101..89889144, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene GRPEL2 pseudogene 1 Neighboring gene uncharacterized LOC105370307 Neighboring gene long intergenic non-protein coding RNA 440 Neighboring gene tripartite motif containing 60 pseudogene 13 Neighboring gene Sp3 transcription factor pseudogene

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

RNA

  1. NR_131229.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL353635, AL354997, BG183515, BG189865, BG191871, BG205744, BG218498
    Related
    ENST00000415193.5

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000013.11 Reference GRCh38.p13 Primary Assembly

    Range
    89214847..89236890 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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